Primary Site >> Stomach Cancer
Gene >> FAM83D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619850 |
| Start | 38952429:38952429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1667C>T |
| AA Mutation | p.Thr556Ile(p.T556I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619850 |
| Start | 38951760:38951760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370045194 |
| CDS Mutation | c.998G>A |
| AA Mutation | p.Arg333Gln(p.R333Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619850 |
| Start | 38951781:38951781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1019C>G |
| AA Mutation | p.Thr340Ser(p.T340S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619850 |
| Start | 38941978:38941978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503A>G |
| AA Mutation | p.Asp168Gly(p.D168G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619850 |
| Start | 38941996:38941996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.521A>T |
| AA Mutation | p.Asp174Val(p.D174V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619850 |
| Start | 38951551:38951551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746962703 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619850 |
| Start | 38951944:38951944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1182G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619850 |
| Start | 38952511:38952511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1749C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000619850 |
| Start | 38952300:38952300(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754952124 |
| CDS Mutation | c.1543delC |
| AA Mutation | p.His515ThrfsTer6(p.H515Tfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |